Meerman Julia J, Ter Hark Sophie E, Janzing Joost G E, Coenen Marieke J H
Department of Psychiatry, Radboud university medical center, Internal mail 966, Geert Grooteplein-Zuid 10, Nijmegen 6500, the Netherland.
Department of Psychiatry, Radboud university medical center, Internal mail 966, Geert Grooteplein-Zuid 10, Nijmegen 6500, the Netherland; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, the Netherland.
J Affect Disord. 2022 May 1;304:1-11. doi: 10.1016/j.jad.2022.02.015. Epub 2022 Feb 11.
Understanding the genetic underpinnings of antidepressant treatment response in unipolar major depressive disorder (MDD) can be useful in identifying patients at risk for poor treatment response or treatment resistant depression. A polygenic risk score (PRS) is a useful tool to explore genetic liability of a complex trait such as antidepressant treatment response. Here, we review studies that use PRSs to examine genetic overlap between any trait and antidepressant treatment response in unipolar MDD.
A systematic search of literature was conducted in PubMed, Embase, and PsycINFO. Our search included studies examining associations between PRSs of psychiatric as well as non-psychiatric traits and antidepressant treatment response in patients with unipolar MDD. A quality assessment of the included studies was performed.
In total, eleven articles were included which contained PRSs for 30 traits. Studies varied in sample size and endpoints used for antidepressant treatment response. Overall, PRSs for attention-deficit hyperactivity disorder, the personality trait openness, coronary artery disease, obesity, and stroke have been associated with antidepressant treatment response in patients with unipolar MDD.
The endpoints used by included studies differed significantly, therefore it was not possible to perform a meta-analysis.
Associations between a PRS and antidepressant treatment response have been reported for a number of traits in patients with unipolar MDD. PRSs could be informative to predict antidepressant treatment response in this population, given advances in the field. Most importantly, there is a need for larger study cohorts and the use of standardized outcome measures.
了解单相重度抑郁症(MDD)中抗抑郁治疗反应的遗传基础,有助于识别治疗反应不佳或难治性抑郁症风险患者。多基因风险评分(PRS)是探索诸如抗抑郁治疗反应等复杂性状遗传易感性的有用工具。在此,我们综述了使用PRS来研究单相MDD中任何性状与抗抑郁治疗反应之间遗传重叠的研究。
在PubMed、Embase和PsycINFO中对文献进行系统检索。我们的检索包括研究单相MDD患者精神及非精神性状的PRS与抗抑郁治疗反应之间的关联。对纳入研究进行质量评估。
总共纳入11篇文章,其中包含30个性状的PRS。研究在样本量和用于抗抑郁治疗反应的终点方面存在差异。总体而言,注意缺陷多动障碍、开放性人格特质、冠状动脉疾病、肥胖和中风的PRS与单相MDD患者的抗抑郁治疗反应相关。
纳入研究使用的终点差异显著,因此无法进行荟萃分析。
已报道单相MDD患者中多个性状的PRS与抗抑郁治疗反应之间存在关联。鉴于该领域的进展,PRS可能有助于预测该人群的抗抑郁治疗反应。最重要的是,需要更大的研究队列并使用标准化结局指标。